| Literature DB >> 21966342 |
Ye Deng1, Young-Won Chin, Hee-Byung Chai, Esperanza Carcache de Blanco, Leonardus B S Kardono, Soedarsano Riswan, Djaja D Soejarto, Norman R Farnsworth, A Douglas Kinghorn.
Abstract
A phytochemical investigation of the leaves of Vitex quinata (Lour.) F.N. Williams (Verbenaceae), guided by the MCF-7 human breast cancer cell line, led to the isolation of a new δ-truxinate derivative (1) and a new phytonoic acid derivative (2), together with 12 known compounds. The structures of the new compounds were determined by spectroscopic methods as dimethyl 3,4,3',4'-tetrahydroxy-δ-truxinate (1) and methyl 10R-methoxy-12-oxo-9(13),16E-phytodienoate (2), respectively. In a cytotoxicity assay, (S)-5-hydroxy-7,4'-dimethoxyflavanone (3) was found to be the sole active principle, with ED(50) values of 1.1-6.7 μM, respectively, when tested against a panel of three human cancer cells. Methyl 3,4,5-O-tricaffeoyl quinate (4) showed activity in an enzyme-based ELISA NF-κB p65 assay, with an ED(50) value of 10.3 μM.Entities:
Year: 2011 PMID: 21966342 PMCID: PMC3182149 DOI: 10.1016/j.phytol.2011.03.007
Source DB: PubMed Journal: Phytochem Lett ISSN: 1874-3900 Impact factor: 1.679